Canonical Allele Identifier: PA2829980332
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238042
ClinVar RCV Id: RCV000227467 RCV003165607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ile1314Asn
CA10583331
NM_021055.3:c.3941T>A